N. Waite, J. Tebby, R. Ward, M. Shaw, Dudley H. Williams
{"title":"膦与乙炔的反应。十四。同分异构体:由三芳基膦和二甲基乙酰二羧酸酯合成的2加合物。一个cyclopentenylidenephosphorane","authors":"N. Waite, J. Tebby, R. Ward, M. Shaw, Dudley H. Williams","doi":"10.1039/J39710001620","DOIUrl":null,"url":null,"abstract":"The reaction of triphenylphosphine and an excess of dimethyl acetylenedicarboxylate gives in addition to the 2H-phosph(V)ole (1), a second product—the cyclopentenylidenephosphorane (2). Reduction of (2) to the dihydro-compound (7) followed by base-catalysed elimination of methanol, gives the cyclopentadienylidenephosphorane (8). The i.r., u.v., n.m.r., and mass spectra of these compounds are discussed.","PeriodicalId":17245,"journal":{"name":"Journal of The Chemical Society C: Organic","volume":"10 1","pages":"1620-1622"},"PeriodicalIF":0.0000,"publicationDate":"1971-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"9","resultStr":"{\"title\":\"Reactions of phosphines with acetylenes. Part XIV. Isomeric 1 : 2 adducts from triarylphosphines and dimethyl acetylenedicarboxylate. A cyclopentenylidenephosphorane\",\"authors\":\"N. Waite, J. Tebby, R. Ward, M. Shaw, Dudley H. Williams\",\"doi\":\"10.1039/J39710001620\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The reaction of triphenylphosphine and an excess of dimethyl acetylenedicarboxylate gives in addition to the 2H-phosph(V)ole (1), a second product—the cyclopentenylidenephosphorane (2). Reduction of (2) to the dihydro-compound (7) followed by base-catalysed elimination of methanol, gives the cyclopentadienylidenephosphorane (8). The i.r., u.v., n.m.r., and mass spectra of these compounds are discussed.\",\"PeriodicalId\":17245,\"journal\":{\"name\":\"Journal of The Chemical Society C: Organic\",\"volume\":\"10 1\",\"pages\":\"1620-1622\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1971-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"9\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of The Chemical Society C: Organic\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1039/J39710001620\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of The Chemical Society C: Organic","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1039/J39710001620","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Reactions of phosphines with acetylenes. Part XIV. Isomeric 1 : 2 adducts from triarylphosphines and dimethyl acetylenedicarboxylate. A cyclopentenylidenephosphorane
The reaction of triphenylphosphine and an excess of dimethyl acetylenedicarboxylate gives in addition to the 2H-phosph(V)ole (1), a second product—the cyclopentenylidenephosphorane (2). Reduction of (2) to the dihydro-compound (7) followed by base-catalysed elimination of methanol, gives the cyclopentadienylidenephosphorane (8). The i.r., u.v., n.m.r., and mass spectra of these compounds are discussed.